Hereditary Spherocytosis (HS) is an inherited blood disorder characterized by the presence of spherocytes—abnormally shaped red blood cells (RBCs) that are sphere-shaped instead of the typical biconcave disc shape.
This condition leads to hemolytic anemia, where RBCs are prematurely destroyed, resulting in a range of symptoms from mild to severe.
Understanding the causes, symptoms, and management of Hereditary Spherocytosis, as well as the crucial role of genetic testing, can help affected individuals and their families navigate this condition more effectively.